Search results for "Metal complex"

showing 10 items of 67 documents

The oxamate route, a versatile post-functionalization for metal incorporation in MIL-101(Cr): Catalytic applications of Cu, Pd, and Au

2013

Abstract A new consecutive post-functionalization method has been developed for the inclusion of additional metal functionalities in Metal Organic Frameworks (MOFs) through oxamate as chelating agent. This may result in catalytic centers of metal–organic complexes or in controlled formation of metal nanoparticles, demonstrated for Cu, Pd and Au, in the highly stable MIL-101(Cr) framework. In a first post-synthesis step, reduction of the NO 2 -MIL-101(Cr) leads to the formation of NH 2 -MIL-101(Cr). The second functionalization consists of a straightforward condensation of the amino groups of the ligand with ethyl chloro-oxoacetate resulting in the formation of free oxamates attached to the …

Heterogeneous catalysisChemistryInorganic chemistrychemistry.chemical_elementHeterogeneous catalysisCopperPost-functionalizationCatalysisCoupling reactionCatalysisMetalMetal complexMetal organic frameworkColloidal goldNH2-MIL-101(Cr)visual_artvisual_art.visual_art_mediumNanoparticlesMetal-organic frameworkOxamateGoldPhysical and Theoretical ChemistryPalladiumCopperPalladium
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Salphen metal complexes as potential anticancer agents: interaction profile and selectivity studies toward the three G-quadruplex units in the KIT pr…

2022

DNA G-rich sequences can organize in four-stranded structures called G-quadruplexes (G4s). These motifs are enriched in significant sites within the human genomes, including telomeres and promoters of cancer related genes. For instance, KIT proto-oncogene promoter, associated with diverse cancers, contains three adjacent G4 units, namely Kit2, SP, and Kitt. Aiming at finding new and selective G-quadruplex binders, we have synthesized and characterized five non-charged metal complexes of Pt(II), Pd(II), Ni(II), Cu(II) and Zn(II) of a chlorine substituted Salphen ligand. The crystal structure of the Pt(II) and Pd(II) complexes was determined by XRPD. FRET measurements indicated that Pt(II) an…

Inorganic ChemistryG-quadruplex Metal complexes SalphenSettore CHIM/03 - Chimica Generale E Inorganica
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Mixed Titanium–Hafnium Chloridometallate Complexes

2007

The addition of either NEt 3 BzCl or [Ph 3 PNPPh 3 ]Cl (1 equiv. chloride per metal) to a 1:1 mixture of HfCl 4 and TiCl 3 in SOCl 2 results in Ti oxidation and leads to the corresponding salts of the [TiHfCl 10 ] 2- ion. A solution IR investigation in the v(M-Cl) region indicates that this ion is in equilibrium with the homodimetallic [Ti 2 Cl 10 ] 2- and [Hf 2 Cl 10 ] 2- ions. An X-ray study of the NEt 3 Bz + salt reveals an edge-sharing bioctahedral dianion sitting on a crystallographic inversion centre. The crystal is a solid solution of different species with compositional disorder at the metal site, each metal position having the occupancy Ti 0.685 Hf 0.315 . The M-M and M-Cl distance…

Inorganic chemistryChloridometallate complexes010402 general chemistryElectrochemistry01 natural sciencesIonlaw.inventionInorganic ChemistryMetalCrystallaw[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM.COOR]Chemical Sciences/Coordination chemistryCrystallizationTitanium010405 organic chemistryChemistryLigandMixed‐metal complexes0104 chemical sciencesCrystallographyOctahedronvisual_artvisual_art.visual_art_mediumHafniumSolid solution
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Weak alkali and alkaline earth metal complexes of low molecular weight ligands in aqueous solution

2008

This work is aimed at reviewing the chemical literature dealing with thermodynamic aspects of the weak complex formation (species with log K values less than about 3) between alkali and alkaline earth metal ions with low molecular weight inorganic and organic ligands in aqueous solution. The following ligands (up to hexavalent anions) were examined in detail: (i) hydroxide, chloride, sulfate, carbonate and phosphate as inorganic, and (ii) carboxylates, amines, amino acids, complexones and nucleotides as organic ligands. The paper also identifies the main reasons responsible for the dispersion of the stability data on ion pairs in the literature. When possible, the trend of stability for the…

Ion pairsSupporting electrolyteMetal ions in aqueous solutionInorganic chemistryAlkali metal complexeWeak complexesChlorideAlkali metal complexes; Alkaline earth metal complexes; Weak complexes; Formation and stability in aqueous solution; Ion pairs.Inorganic Chemistrychemistry.chemical_compoundAlkali metal complexesAlkaline earth metal complexesMaterials ChemistrymedicineFormation and stability in aqueous solutionSettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistryWeak complexeAlkaline earth metalAqueous solutionChemistryLigandAlkali metalAlkaline earth metal complexeHydroxidemedicine.drugCoordination Chemistry Reviews
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Fluorescent metal-based complexes as cancer probes.

2020

Abstract The ability to track drugs inside of cells and tumours has been highly valuable in cancer research and diagnosis. Metal complexes add attractive features to fluorescent drugs, such as targeting and specificity, solubility and uptake or photophysical properties. This review focuses on the latest fluorescent metal-based complexes, their cellular targets, photophysical properties and possible anticancer effects.

LightClinical BiochemistryPharmaceutical ScienceAntineoplastic Agents01 natural sciencesBiochemistryMetal-based probesMetalMetal complexesCoordination ComplexesCell Line TumorMetals HeavyNeoplasmsDrug DiscoveryAnticancer probesFluorescence microscopemedicineAnimalsHumansSolubilityMolecular BiologyFluorescent DyesFluorescence microscopyTargeting010405 organic chemistryChemistryOrganic ChemistryCancermedicine.diseaseTheranosticsCombinatorial chemistryFluorescence0104 chemical sciences010404 medicinal & biomolecular chemistryvisual_artvisual_art.visual_art_mediumFluorescent probesMolecular MedicineBioorganicmedicinal chemistry letters
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A novel 2,6-bis(benzoxazolyl)phenol macrocyclic chemosensor with enhanced fluorophore properties by photoinduced intramolecular proton transfer

2023

Macrocyclic ligand L, in which a 2,6-bis(2-benzoxazolyl)phenol (bis-HBO) group is incorporated in triethylenetetramine, was designed and synthesized with the aim of creating a chemosensor with high selectivity and specificity for metal cations in an aqueous environment. The availability of several proton acceptors and donors, and amine and phenol hydroxy groups, respectively, affects the keto-enol equilibrium in both the ground and excited states, and the ligand properties show dependence on the pH of the solution. L is fluorescent in the visible range, through an excited-state intramolecular proton transfer (ESIPT) mechanism. The results of an exhaustive characterization of L by spectrosco…

Macrocyclic ligandInorganic ChemistryExcited state intramolecular proton transfer (ESIPT)Settore CHIM/03 - Chimica Generale E InorganicaFluorescence sensorDFT calculationMetal complexeDalton Transactions
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Coordination Complexes of a Neutral 1,2,4-Benzotriazinyl Radical Ligand: Synthesis, Molecular and Electronic Structures, andMagnetic Properties

2015

A series of d-block metal complexes of the recently reported coordinating neutral radical ligand 1-phenyl-3-(pyrid-2-yl)-1,4-dihydro-1,2,4-benzotriazin-4-yl (1) was synthesized. The investigated systems contain the benzotriazinyl radical 1 coordinated to a divalent metal cation, MnII, FeII, CoII, or NiII, with 1,1,1,5,5,5-hexafluoroacetylacetonato (hfac) as the auxiliary ligand of choice. The synthesized complexes were fully characterized by single-crystal X-ray diffraction, magnetic susceptibility measurements, and electronic structure calculations. The complexes [Mn(1)(hfac)2] and [Fe(1)(hfac)2] displayed antiferromagnetic coupling between the unpaired electrons of the ligand and the meta…

Magnetic susceptibility measurementsAntiferromagnetic couplingIron compoundsLigands01 natural sciencesNickelheterosyklitMetal ionsta116Cobalt compoundsChelationChemistryMetal–radical interactionsMagnetismSingle crystal x-ray diffractionRadicals[CHIM.MATE]Chemical Sciences/Material chemistrymetal-radical interactionsradicalsexchange interactionsChemistrykoordinaatiokemiaUnpaired electronPositive ionsMetalsSynthesis (chemical)visual_artradikaalitvisual_art.visual_art_mediumElectronic structureCoordinating propertiesmagneettiset ominaisuudetX ray diffractionRadicalInorganic chemistryRadical interactionsElectronic structureHeterocycles010402 general chemistryCatalysisMagnetic susceptibilityMetalElectronic structure calculationsMetal complexesMagnetic properties[CHIM.COOR]Chemical Sciences/Coordination chemistrymetalli-radikaali -vuorovaikutuksetManganeseheterocycles010405 organic chemistryLigandCrystal structureOrganic ChemistryGeneral ChemistryMagnetic susceptibility0104 chemical sciencesCrystallographyOctahedronFerromagnetismExchange interactionscoordination chemistrySingle crystalsmagnetic propertiesCoordination reactions
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Flexible light-emitting electrochemical cells with single-walled carbon nanotube anodes

2016

Abstract In this work, we demonstrate flexible solution processed light emitting electrochemical cells (LECs) which use single-walled carbon nanotubes (SWCNTs) films as the substrate. The SWCNTs were synthesized by an integrated aerosol method and dry-transferred on the plastic substrates at room temperature. The addition of a screen printed poly (3,4-ethylene dioxythiophene) doped with poly (styrene sulfonate) (PEDOT:PSS) film onto the nanostructured electrode further homogenizes the surface and enlarges the work function, enhancing the hole injection into the active layer. By using an efficient phosphorescent ionic transition metal complex (iTMC) as the active material, efficacies up to 9…

Materials scienceLight-emitting electrochemical cellsFlexible devices02 engineering and technologySubstrate (electronics)Carbon nanotubeElectroluminescence010402 general chemistry01 natural sciencesElectrochemical celllaw.inventionBiomaterialsPEDOT:PSSlawSWCNTsMaterials ChemistryOLEDWork functionElectrical and Electronic Engineeringta114business.industryOLEDsGeneral ChemistryTransition metal complex021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesElectronic Optical and Magnetic MaterialsElectroluminescenceElectrodeOptoelectronics0210 nano-technologybusinessORGANIC ELECTRONICS
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The solution behavior of dopamine in the presence of mono and divalent cations: A thermodynamic investigation in different experimental conditions

2021

The interactions of dopamine [2-(3,4-Dihydroxyphenyl)ethylamine, (Dop-)] with methylmercury(II) (CH3Hg+), magnesium(II), calcium(II), and tin(II) were studied in NaCl(aq) at different ionic strengths and temperatures. Different speciation models were obtained, mainly characterized by mononuclear species. Only for Sn2+ we observed the formation of binuclear complexes (M2L2 and M2LOH (charge omitted for simplicity)

Models MolecularCations DivalentDopaminePotentiometric titrationEnthalpyIonic bondingBiochemistryMicrobiologyArticleDivalentchemistry.chemical_compoundMetal complexesTheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYSettore CHIM/01 - Chimica AnaliticaStability constantsMolecular Biologychemistry.chemical_classificationCatechol; Chemical speciation; Metal complexes; Sequestration; Stability constantsLigandHydrolysisOsmolar ConcentrationTemperatureSequestrationHydrogen-Ion ConcentrationQR1-502SolutionsKineticschemistrySpecific ion interaction theoryIonic strengthThermogravimetryCatecholPhysical chemistryThermodynamicsChemical speciationEthylamine
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Synthesis, characterization, cellular uptake and interaction with native DNA of a bis(pyridyl)-1,2,4-oxadiazole copper(II) complex

2010

The copper(II) complex of 3,5-bis(2'-pyridyl)-1,2,4-oxadiazole was synthesized and characterized. X-Ray crystallography revealed that the complex consists of a discrete [Cu(3,5-bis(2'-pyridyl)-1,2,4-oxadiazole)(2)(H(2)O)(2)](2+) cation and two ClO(4)(-) anions. The Cu(II) coordination sphere has a distorted octahedral geometry and each ligand chelates the copper ion through the N(4) nitrogen of the oxadiazole ring and the nitrogen of one pyridine moiety. The coordinated water molecules are in cis position and each of them is H-bonded to the 5-pyridyl nitrogen of the oxadiazole ligand and to an oxygen of the perchlorate anion. Biological assays showed that, despite the free ligand not being …

Models MolecularCircular dichroismCoordination sphereheterocylces metal complex DNA binders anti-tumoralsCell SurvivalPyridinesStereochemistrychemistry.chemical_elementOxadiazoleLigandsInorganic Chemistrychemistry.chemical_compoundPerchlorateCell Line TumorOctahedral molecular geometryOrganometallic CompoundsHumansOxadiazolesChemistryLigandDNASettore CHIM/06 - Chimica OrganicaCopperBinding constantCrystallographySettore CHIM/03 - Chimica Generale E InorganicaCopper
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